A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899117



Internal ID22674243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186311820..186312155hg38UCSC Ensembl
chr3:186029609..186029944hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17422823
Samples
Known GenesDGKG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899117
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer